Product Recalls in Indiana

Product recalls affecting Indiana — including food, drugs, consumer products, medical devices, and vehicles distributed to Indiana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,101 recalls have been distributed to Indiana in the last 12 months.

53,528 total recalls
1,101 in last 12 months

Showing 13521–13540 of 53,528 recalls

Medical DeviceFebruary 25, 2022· Qiagen Sciences LLC

Recalled Item: therascreen KRAS RGQ PCR Kit (24) Model Number(s): (US IVD) Recalled by...

The Issue: False positive or false negative G12C (12CYS) mutation result for the KRAS...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono floor in combination with a Siemens Healthineers table Recalled...

The Issue: Five potential software issues affecting Artis pheno and Artis icono systems...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Philips North America Llc

Recalled Item: DigitalDiagnost C50 1.1 Recalled by Philips North America Llc Due to...

The Issue: Following a system restart where the Table Height 2 (TH2) is the default...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 25, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo Application software VE20 (Material Number 10848815) installed on the...

The Issue: After CT image data from Toshiba is loaded, image mirroring can occur along...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 25, 2022· Damascus Bakery LLC

Recalled Item: Damascus Bakery Recalled by Damascus Bakery LLC Due to Undeclared Egg

The Issue: Undeclared Egg Allergen

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 25, 2022· B. Braun Medical, Inc.

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical, Inc. Due to...

The Issue: Lack of sterility assurance: leaking bags

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2022· The Harvard Drug Group

Recalled Item: hydrALAZINE HCl Tablets Recalled by The Harvard Drug Group Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification result...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR System Recalled by Boston Scientific Corporation Due to Users need...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· ROi CPS LLC

Recalled Item: Regard Custom Procedure Kits containing BD Luer Lok Access Devices Recalled...

The Issue: Recalled devices were packaged in convenience kits.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceFebruary 24, 2022· International Science & Technology, LP, DBA Diamatrix Ltd.

Recalled Item: Outer Packaging Label: Protekt Sharps Safety Knives - 44620MU Recalled by...

The Issue: Surgical knives may contain incorrect description printed on handles....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 24, 2022· Boston Scientific Corporation

Recalled Item: SpaceOAR Vue System Recalled by Boston Scientific Corporation Due to Users...

The Issue: Users need to be aware that embolism is a possible adverse event associated...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee multi-purpose Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor Recalled by Siemens Medical Solutions USA, Inc Due to If the...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen floor Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 23, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee ceiling Recalled by Siemens Medical Solutions USA, Inc Due to If...

The Issue: If the coolant level in the cooling circuit drops below a certain level,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing